🏥 VAERS Vaccine Data Browser

🔒 Privacy & Data Disclaimer

About This Site

This is a public data browser for the Vaccine Adverse Event Reporting System (VAERS). By using this site, you acknowledge and agree to the following:

Data Source & Accuracy

  • Public Data: All data displayed comes from the publicly available VAERS database maintained by the CDC and FDA.
  • No Verification: VAERS accepts all reports without verifying medical accuracy. Reports do not prove causation between vaccines and adverse events.
  • Anyone Can Report: Healthcare providers, patients, family members, and anyone else can submit reports to VAERS.
  • Research Purpose: This data is for transparency, research, and monitoring vaccine safety signals only.

Your Privacy

  • No Personal Data Collection: This site does not collect, store, or track any personal information about visitors.
  • No Cookies: We do not use cookies except for remembering that you've seen this disclaimer (stored locally in your browser).
  • No Analytics: We do not use Google Analytics or any other tracking services.
  • Search Privacy: Your searches and filters are not logged or stored on our servers.
  • Public Data Only: The VAERS data shown here is already public and contains no personally identifiable information.

Medical Disclaimer

  • Not Medical Advice: This tool is for informational purposes only and does not provide medical advice.
  • Consult Healthcare Providers: Always consult qualified healthcare professionals for medical decisions.
  • No Liability: We are not responsible for decisions made based on this data.

Data Interpretation

  • The presence of a report does not mean the vaccine caused the adverse event.
  • Coincidental events are often reported (e.g., a heart attack that happened to occur after vaccination).
  • Serious adverse events must be reported by law, even if unrelated to the vaccine.
  • The database is useful for detecting safety signals that require further investigation.

📖 Help & Search Guide

Column Icons Legend

💀 Death
🏥 Hospitalized
🚑 Emergency Room
♿ Disability
⚠️ Life Threatening

How to Search

💡 Search Tips:
  • Select Year: Choose a specific year OR "All Years" to search across all data
  • All Years requires filters: When searching all years, you must select at least one filter (lot number, vaccine type, outcome, etc.) for performance
  • Lot number tracking: Use "All Years" + Lot Number to track lots across multiple years
  • Combine filters: Use multiple filters together to narrow results (e.g., Age + Vaccine Type + Death)
  • VAERS ID: Search for specific report by ID number
  • Age: Enter exact age (e.g., 25) or decimal (e.g., 0.5 for 6 months)
  • State: Enter 2-letter state code (e.g., CA, NY, TX)
  • Vaccine Type: Search partial names (e.g., "COVID19", "FLU", "HPV")
  • Manufacturer: Search by company (e.g., "PFIZER", "MODERNA")
  • Lot Number: Search specific vaccine lot (works great with "All Years")
  • Symptoms: Search for any symptom keyword (e.g., "fever", "rash")
  • Death/Hospitalized: Filter to only show cases with these outcomes

Understanding the Data

  • Reports are unverified: VAERS accepts all reports without medical verification
  • Not proof of causation: A report does not mean the vaccine caused the event
  • Anyone can report: Healthcare providers, patients, and family members can submit reports
  • Multiple vaccines: One report may list multiple vaccines given at the same time
  • Blank fields: Not all fields are required, so some data may be missing

Using the Table

  • Sort columns: Click column headers (ID, Age, Sex, Date, Died) to sort
  • Expand text: Click "More" to see full narrative or symptom text
  • Navigate pages: Use pagination controls at top and bottom of table
  • Export results: Click "📥 Export CSV" to download filtered data (max 10,000 records)

💡 Frequently Asked Questions (FAQ)

What is this site?

🏥 VAERS Vaccine Data Browser is an independent, third-party data browser for publicly available VAERS (Vaccine Adverse Event Reporting System) data.

Important: This site is NOT affiliated with, endorsed by, or operated by the CDC, FDA, or any government agency. We are an independent service that makes public VAERS data easier to search and analyze.

What is VAERS?

VAERS (Vaccine Adverse Event Reporting System) is a national early warning system established in 1990 to detect possible safety problems with vaccines. It's co-managed by the CDC (Centers for Disease Control and Prevention) and FDA (Food and Drug Administration).

VAERS accepts and analyzes reports of adverse events (possible side effects) after a person has received a vaccination.

Official VAERS website: vaers.hhs.gov

Is this data HIPAA compliant?

Yes, absolutely. All VAERS data displayed here is:

  • Publicly available - Published by the CDC/FDA on their official website
  • De-identified - Contains no personally identifiable information (names, addresses, contact info removed)
  • Legally accessible - Available to researchers, media, and the general public under FOIA (Freedom of Information Act)
  • Not protected health information - Once de-identified and published by the government, it's no longer covered by HIPAA restrictions

This site displays the same public data available at vaers.hhs.gov/data.

Why does this site exist?

We believe in transparency and public access to health data. While the CDC/FDA provide VAERS data, their official site:

  • Is difficult to search and filter
  • Requires downloading large CSV files and technical knowledge
  • Is not user-friendly for the average person

This independent site makes the same publicly available data easier to search, filter, and understand for researchers, journalists, healthcare workers, and concerned citizens.

Where does the data come from?

All data is downloaded directly from the official CDC/FDA VAERS website at vaers.hhs.gov/data.

The data is:

  • Publicly released by the CDC/FDA every week
  • Available as downloadable CSV files
  • Imported into this site's database for easier searching
  • Displayed exactly as provided (no modifications or filtering)

This site does not collect, modify, or add to the official VAERS data.

My vaccine lot number matches one with deaths/serious events - should I be worried?

Important context:

  • VAERS reports do NOT prove causation - A report means an event occurred after vaccination, but doesn't mean the vaccine caused it
  • Anyone can report - Reports are not verified for medical accuracy before being published
  • Coincidences happen - When millions of people get vaccinated, some will experience unrelated medical events afterward
  • Large lot numbers - Popular vaccines may have hundreds of thousands of doses from one lot number
  • More vaccinations = more reports - Lots used widely will naturally have more reports

What to do:

  • Don't panic - VAERS data requires expert analysis to interpret
  • Talk to your doctor if you have concerns
  • Check official CDC/FDA safety communications for genuine safety signals
  • Remember: billions of vaccine doses have been safely administered

Can I trust VAERS data?

VAERS is valuable but has limitations:

Strengths:

  • ✅ Early warning system for potential safety signals
  • ✅ Open and transparent - publicly accessible
  • ✅ Accepts all reports regardless of likelihood of causation
  • ✅ Monitored by CDC/FDA experts who investigate concerning patterns

Limitations:

  • ⚠️ Reports are unverified - not investigated before publication
  • ⚠️ Cannot determine if vaccine caused the event
  • ⚠️ Underreporting - not all adverse events are reported
  • ⚠️ Overreporting - coincidental events may be reported
  • ⚠️ Incomplete data - not all fields are required

Bottom line: VAERS is an important tool for safety monitoring, but individual reports should not be used as proof that a vaccine caused harm.

What are "adverse events"?

An adverse event is any undesirable health occurrence that happens after vaccination, including:

  • Common reactions: Sore arm, mild fever, fatigue (usually expected)
  • Serious events: Hospitalization, disability, life-threatening illness, death
  • Coincidental events: Medical conditions that would have occurred anyway

Important: An adverse event doesn't mean the vaccine caused it - only that it occurred after vaccination. Many reported events are coincidental or unrelated.

Why are some lot numbers listed multiple times?

This is normal and expected! A person may receive multiple doses of the same vaccine from the same lot number:

  • COVID vaccines require 2-3 doses
  • HPV, Hepatitis B, and other vaccines have multi-dose schedules
  • Each dose is recorded as a separate entry

Example: Person receives Pfizer COVID dose 1 (lot ABC123) and dose 2 (lot ABC123) - lot ABC123 appears twice in their report.

How often is this data updated?

The CDC/FDA releases new VAERS data every Friday. This site is typically updated:

  • Weekly or bi-weekly for recent data
  • Check the available years to see what data is currently loaded
  • During updates, the site may be in maintenance mode temporarily

Where can I learn more?

⚠️ DISCLAIMER: This data is from the Vaccine Adverse Event Reporting System (VAERS). Reports do not establish causation between vaccines and adverse events. Anyone can submit a report, and reports are not verified. This is raw data for transparency and research purposes only.
34,052
Total Reports (2025)
500
Deaths Reported
1,634
Hospitalizations
30
ER Visits
1,191
Disabilities
570
Life Threatening
🔄 Reset 📥 Export CSV
ID Age Sex State Date ▼ Onset Days Vaccine Manufacturer Lot # Symptoms Narrative 💀 🏥 🚑 ♿ ⚠️
2873132 51 M 11/17/2025 COVID19
 MODERNA
Arthralgia, Carpal tunnel syndrome, Condition aggravated, Mobility decreased Arthralgia, Carpal tunnel syndrome, Condition aggravated, Mobility decreased
carpal tunnel in right wrist exacerbation with joint pain and limited range of motion carpal tunnel in right wrist exacerbation with joint pain and limited range of motion
2873133 68 M CT 11/17/2025 FLU3
 SEQIRUS, INC.
Arthralgia, Injected limb mobility decreased, Pain Arthralgia, Injected limb mobility decreased, Pain
Patient called on 11/17/25 reported that he has had shoulder pain since the day after getting the f... Patient called on 11/17/25 reported that he has had shoulder pain since the day after getting the flu shot which was on 9/30/25. He is having trouble lifting and has decreased range of motion. Reported pain level is 6 out of 10 with certain movement More
2873134 83 F TX 11/17/2025 COVID19
 MODERNA
Mobility decreased Mobility decreased
per pt woke up morning after immunization, had to go to ER because "could not move" per pt woke up morning after immunization, had to go to ER because "could not move"
2873138 18 F 11/17/2025 FLU3
 SANOFI PASTEUR
 u8881da
Unevaluable event Unevaluable event
None None
2873139 32 M CA 11/17/2025 COVID19
 MODERNA
Bipolar I disorder, Condition aggravated, Mania Bipolar I disorder, Condition aggravated, Mania
Mania developed in patient with bipolar disorder Mania developed in patient with bipolar disorder
2873142 18 F 11/17/2025 COVID19
FLU3
 PFIZER\BIONTECH
SANOFI PASTEUR
 na0590
u8832da
Syncope; Syncope Syncope; Syncope
After receiving both vaccines, the patient fainted about 7 seconds. Per patient, she is anemic that ... After receiving both vaccines, the patient fainted about 7 seconds. Per patient, she is anemic that she is prone to faint (normally faints after blood draw) however it was her first time fainting after vaccinations. The patient was with her parents at the time of vaccination and stayed about 15 minutes in a separate counseling room and follow up on the next day via phone call on which the patient stated that she is doing well. More
2873145 73 M FL 11/17/2025 FLU3
 SANOFI PASTEUR
 U8764CB
Hypoaesthesia, Paraesthesia Hypoaesthesia, Paraesthesia
Numbness in hand and tingling in fingers of left arm which I received the vaccine approximately 2 ho... Numbness in hand and tingling in fingers of left arm which I received the vaccine approximately 2 hours after the injection. This continued for 4-6 hours. More
2873146 63 M TX 11/17/2025 FLU3
 SANOFI PASTEUR
 UT8873JA
Cough, Hypoaesthesia, Wheezing Cough, Hypoaesthesia, Wheezing
approx 10 minutes post injection patient stated he felt "funny", numbness on left side of ... approx 10 minutes post injection patient stated he felt "funny", numbness on left side of face. Patient then developed audible wheezing, uncontrolled coughing within 20 minutes of receiving vaccine. Physician notified, albuterol nebulizer treatment given, 40 mg solumedrol IM given. Post treatment patient with wheezing resolved, patient then developed paroxysmal coughing. Physician notified of new symptom, 911 called. Upon arrival of EMS, coughing subsided, patient declined to have EC evaluation More
2873147 72 F MO 11/17/2025 FLU3
 SEQIRUS, INC.
 407276
Immediate post-injection reaction, Injection site bruising, Injection site haemo... Immediate post-injection reaction, Injection site bruising, Injection site haemorrhage More
Immediately following administration into left deltoid, a small amount of blood came from the site o... Immediately following administration into left deltoid, a small amount of blood came from the site of administration and was stopped after approximately 1 minute by applying pressure to the site with a cotton ball. A small, approximately dime-sized area of presumed bruising was seen under the skin immediately around the site of administration. I advised the patient to wait in the pharmacy for 15 minutes for monitoring, but she refused noting that she had an appointment to get to. More
2873148 42 F OR 11/17/2025 COVID19
FLU3
 PFIZER\BIONTECH
SEQIRUS, INC.
 NA4457
948402
Chest discomfort, Dizziness, Dyspnoea, Throat irritation, Throat tightness; Ches... Chest discomfort, Dizziness, Dyspnoea, Throat irritation, Throat tightness; Chest discomfort, Dizziness, Dyspnoea, Throat irritation, Throat tightness More
Patient reportedly received both the influenza and Pfizer Covid vaccines in her right deltoid around... Patient reportedly received both the influenza and Pfizer Covid vaccines in her right deltoid around 0940 this morning in the doctor's office. Patient reportedly developed chest pressure, mild shortness of breath, throat tightness and itching, and lightheadedness about 3 minutes after the injections. Patient was assessed by RN immediately and initial vitals were BP 145/83, HR 90, SpO2 100% on room air. Patient remained alert and oriented, in no respiratory distress, speaking clearly and coherently in full phrases. Provider assessed patient who had a reassuring exam. Patient reportedly was feeling much better after a few minutes of resting, however was given one dose of Benadryl 25 mg orally due to throat itchiness. Patient's vitals re-checked and returned to baseline -- BP 128/85, HR 56, and SpO2 100% at room air. Patient confirmed symptoms improved and was comfortable with discharge after being monitored for 20 minutes. Patient with steady gait and discharged without incident and given ER precautions. More
2873149 60 F TN 11/17/2025 FLU3
 SANOFI PASTEUR
 U8863BA
Anxiety, Chest discomfort, Ocular hyperaemia, Paraesthesia, Tinnitus Anxiety, Chest discomfort, Ocular hyperaemia, Paraesthesia, Tinnitus
Bloodshot eyes, ringing in the ears, tingling in face, brief heaviness in chest when walking up stai... Bloodshot eyes, ringing in the ears, tingling in face, brief heaviness in chest when walking up stairs, and feeling anxious. More
2873151 73 F OR 11/17/2025 COVID19
 MODERNA
 3052549
Arthralgia Arthralgia
Patient has had shoulder pain since the day after vaccine administration. Patient has had shoulder pain since the day after vaccine administration.
2873152 77 M VA 11/17/2025 COVID19
 MODERNA
Asthenia, Feeling cold, Mobility decreased, Tremor Asthenia, Feeling cold, Mobility decreased, Tremor
about 10 hours later I started violently shaking. I was cold and couldn't sit up. My wife could... about 10 hours later I started violently shaking. I was cold and couldn't sit up. My wife couldn't even pull me up. Its like my back would not move, but I could move my limbs. These symptoms lasted most of the night. It took about 4 days before I felt better. More
2873154 75 M TX 11/17/2025 FLUN3
 MEDIMMUNE VACCINES, INC.
 u8859ba
Anaphylaxis treatment, Dizziness, Eye movement disorder, Hypopnoea Anaphylaxis treatment, Dizziness, Eye movement disorder, Hypopnoea
patient felt dizzy and swallow breathing with rolling eyes after shot was given by a certified IMZ t... patient felt dizzy and swallow breathing with rolling eyes after shot was given by a certified IMZ technician. Had to be given 1 shot of Epipen . More
2873155 82 M NJ 11/17/2025 COVID19
 MODERNA
 3052296
Pain, Shoulder injury related to vaccine administration Pain, Shoulder injury related to vaccine administration
Patient is self reporting potential SIRVA on 11/17/2025. States difficulty lifting arm without pain Patient is self reporting potential SIRVA on 11/17/2025. States difficulty lifting arm without pain
2873157 3 M MD 11/17/2025 FLU3
 SEQIRUS, INC.
Cellulitis, Erythema, Pain, Rash Cellulitis, Erythema, Pain, Rash
Rash, erythema, cellulitis area affected larger than 10cm, pain Rash, erythema, cellulitis area affected larger than 10cm, pain
2873158 77 F MN 11/17/2025 FLU3
 SANOFI PASTEUR
 UT8763EA
Injection site bruising Injection site bruising
Patient received flu shot on 11/12/25. On 11/17, she presented to pharmacy with a Dark blue/purple/b... Patient received flu shot on 11/12/25. On 11/17, she presented to pharmacy with a Dark blue/purple/black bruise across her arm where injection was given - about 2.5 inches up and down and 5 inches across. Yellow around edges of bruise. Does not hurt or burn. It has grown in size over the last couple of days. More
2873160 71 F MI 11/17/2025 COVID19
FLU3
 MODERNA
SEQIRUS, INC.
 3053777
407274
Influenza like illness, Injection site bruising, Injection site pain, Wrong tech... Influenza like illness, Injection site bruising, Injection site pain, Wrong technique in product usage process; Influenza like illness, Injection site bruising, Injection site pain, Wrong technique in product usage process More
Patient stated that she developed a very large, dark bruise after receiving two vaccines in her righ... Patient stated that she developed a very large, dark bruise after receiving two vaccines in her right arm. She first noticed the bruise about 3 days later, and says that it was black in color and approximately 4 inches in diameter. She said that she had a second, smaller bruise about 1/4 inch apart from the large bruise. The second bruise was much lighter in color, and about 1.5 inches in diameter. Patient stated that the immunizer held her arm up very high before administering, and that the vaccines were "rough." Patient saw her primary care physician on 11/17/25, and showed him the bruise; which was still present 12 days later. They physician acknowledged that it was abnormal to bruise to that extent after a vaccine, but did not provide any additional comments or instruction. According to the patient, the bruise is now approximately 2.5 inches in diameter and has faded to a blotchy purple color. Patient states that the bruise continues to improve every day and she has been instructed to monitor it. Patient also stated that her arm is still tender, and was instructed to notify the pharmacy or physician if this worsens or does not improve. Additionally, patient developed mild, flu like symptoms for about a day and a half after being immunized. More
2873162 10 F CO 11/17/2025 COVID19
 PFIZER\BIONTECH
 NA0846
Anxiety, Condition aggravated, Syncope Anxiety, Condition aggravated, Syncope
anxiety fainted anxiety fainted
2873163 23 M CA 11/17/2025 COVID19
COVID19
HPV9
HPV9
 MODERNA
MODERNA
MERCK & CO. INC.
MERCK & CO. INC.



Chest discomfort, Dry eye, Dry mouth, Injection site pain, Malaise; Pain in extr... Chest discomfort, Dry eye, Dry mouth, Injection site pain, Malaise; Pain in extremity, Somnolence; Chest discomfort, Dry eye, Dry mouth, Injection site pain, Malaise; Pain in extremity, Somnolence More
A few hours after registering for the vaccine, I felt unwell in my heart, tired, and drowsy, so I we... A few hours after registering for the vaccine, I felt unwell in my heart, tired, and drowsy, so I went to bed at 8 p.m. that night. The next morning, my legs ached, and the injection site in my left arm was still painful. I felt chest tightness and discomfort during the day. My eyes and mouth were dry while I slept at night. More
2873167 71 F 11/17/2025 FLU3
 SANOFI PASTEUR
 ut8794ca
Dizziness, Injection site pruritus, Injection site reaction, Urticaria Dizziness, Injection site pruritus, Injection site reaction, Urticaria
Patient reported dizziness on drive home. then around 3 hours later her arm that she had the flu sho... Patient reported dizziness on drive home. then around 3 hours later her arm that she had the flu shot in became itchy and a welt under the injection site. Patient took a Benadryl. I called patient in morning, she reported itching had stopped but later that night she had developed hives under her arm and waist. she stated that the hives were gone that morning. More
2873170 0.33 F OK 11/17/2025 DTAPHEPBIP
PNC20
RV1
 GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
 9P329
LX2496
EX434
No adverse event, Wrong product administered; No adverse event, Wrong product ad... No adverse event, Wrong product administered; No adverse event, Wrong product administered; No adverse event, Wrong product administered More
No adverse s/s noted by parents, patient was intended to get DTaP-IPV-Hib (Pentacel) but was given D... No adverse s/s noted by parents, patient was intended to get DTaP-IPV-Hib (Pentacel) but was given DTaP-HepB-IPV (Pediarix). More
2873172 91 M CA 11/17/2025 FLU3
 SANOFI PASTEUR
 U8874Aa
Extra dose administered, No adverse event Extra dose administered, No adverse event
On November 17, 2025, the patient presented to our retail pharmacy to receive a high-dose influenza ... On November 17, 2025, the patient presented to our retail pharmacy to receive a high-dose influenza (HD flu) vaccination. The pharmacist had previously consulted with the patient in October 2025, during which the patient elected to postpone vaccination until November based on the timing of his influenza immunization from the prior year. Upon the patient?s arrival, the pharmacist accessed and printed the patient?s record from the state Immunization Registry to review current immunization status and determine if any additional vaccines were due. Following administration of the HD flu vaccine, the pharmacist proceeded to document the dose in state system and subsequently noted that an existing record indicated the patient had already received an influenza vaccination at another location in October 2025. The duplicate administration was unintentional and identified immediately upon documentation review. The patient remained in the pharmacy for observation and exhibited no adverse reactions at the time of reporting. More
2873173 56 F MT 11/17/2025 COVID19
 MODERNA
 3053777
Chills, Fatigue, Oral herpes Chills, Fatigue, Oral herpes
EXTREME FATIGUE, RIGORS, AND HIGH FEVER (FIRST MEASURED 103+* AROUND 3AM 11/17/25), FEVER CURRENTLY ... EXTREME FATIGUE, RIGORS, AND HIGH FEVER (FIRST MEASURED 103+* AROUND 3AM 11/17/25), FEVER CURRENTLY AT 101* AS OF 4 PM 11/17/25. More
2873185 F 11/17/2025 VARZOS
 GLAXOSMITHKLINE BIOLOGICALS
 7523J
Fatigue, Oropharyngeal blistering, Oropharyngeal pain Fatigue, Oropharyngeal blistering, Oropharyngeal pain
Sore throat full of blisters like shingles; Sore throat; Fatigue; This serious case was reported by ... Sore throat full of blisters like shingles; Sore throat; Fatigue; This serious case was reported by a consumer and described the occurrence of throat blister in a 61-year-old female patient who received Herpes zoster (Shingrix) (batch number 7523J, expiry date 06-NOV-2026) for prophylaxis. On 06-NOV-2025, the patient received Shingrix. On 07-NOV-2025, 1 days after receiving Shingrix, the patient experienced throat blister (Verbatim: Sore throat full of blisters like shingles) (serious criteria GSK medically significant) and sore throat (Verbatim: Sore throat). In NOV-2025, the patient experienced fatigue (Verbatim: Fatigue). The outcome of the throat blister and sore throat were unknown and the outcome of the fatigue was not reported. It was unknown if the reporter considered the throat blister, sore throat and fatigue to be related to Shingrix. The company considered the throat blister to be unrelated to Shingrix. It was unknown if the company considered the sore throat and fatigue to be related to Shingrix. Additional Information: GSK Receipt Date: 08-NOV-2025 Patient had sore throat full of blisters like shingles. Fatigue and sores was just resting and took fluids.; Sender's Comments: A case of Oropharyngeal blistering, 1 days after receiving Shingrix, in a 61-year-old female patient. Based on the available information a possible causality that the event was caused by GSK vaccine product cannot be ascertained. Consent for further follow up has not been received. More
2873197 11/17/2025 VARZOS
VARZOS
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
 UNK
UNK
Herpes zoster, Hip arthroplasty, Vaccination failure; Herpes zoster, Hip arthrop... Herpes zoster, Hip arthroplasty, Vaccination failure; Herpes zoster, Hip arthroplasty, Vaccination failure More
they got activated when you got your surgery/ suspected vaccination failure; Hip replacement; they g... they got activated when you got your surgery/ suspected vaccination failure; Hip replacement; they got activated when you got your surgery; This serious case was reported by a consumer via interactive digital media and described the occurrence of vaccination failure in a patient who received Herpes zoster (Shingles vaccine) for prophylaxis. Co-suspect products included Herpes zoster (Shingles vaccine) for prophylaxis. On an unknown date, the patient received the 2nd dose of Shingles vaccine and the 1st dose of Shingles vaccine. On an unknown date, an unknown time after receiving Shingles vaccine and Shingles vaccine, the patient experienced vaccination failure (Verbatim: they got activated when you got your surgery/ suspected vaccination failure) (serious criteria GSK medically significant), hip replacement (Verbatim: Hip replacement) (serious criteria clinically significant/intervention required) and shingles (Verbatim: they got activated when you got your surgery). The outcome of the vaccination failure, hip replacement and shingles were not reported. It was unknown if the reporter considered the vaccination failure, hip replacement and shingles to be related to Shingles vaccine. It was unknown if the reporter considered the vaccination failure and shingles to be related to Shingles vaccine. The company considered the vaccination failure and hip replacement to be unrelated to Shingles vaccine and Shingles vaccine. It was unknown if the company considered the shingles to be related to Shingles vaccine and Shingles vaccine. Additional Information: GSK Receipt Date: 11-NOV-2025 This case was reported by a patient via interactive digital media. The patient got both vaccine 3 years ago and when he/she had a hip replacement a year and a half, he/she had them but his/her doctor said that they got activated when he/she got surgery. Patient reported that it was the worse and was under a treatment for 14 days. The follow-up could not be possible as no contact details were available. This case was considered as suspected vaccination failure as details regarding time to onset and laboratory test confirming shingles were unknown at the time of reporting. The batch number was not provided, and we are unable to contact the reporter.; Sender's Comments: A case of Vaccination failure and Hip arthroplasty, unknown time after receiving Shingles vaccine( 1st and 2nd ), in a patient. Based on the available information a? possible causality that the event was caused by the GSK product cannot be ascertained. Consent for further follow-up has not been received. More
2873202 F NJ 11/17/2025 DTAP
DTAP
DTAP
FLUX
FLUX
FLUX
 UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
UNKNOWN MANUFACTURER
 UNK
UNK
UNK
UNK
UNK
UNK
Antinuclear antibody positive, Arthralgia, Double stranded DNA antibody positive... Antinuclear antibody positive, Arthralgia, Double stranded DNA antibody positive, Full blood count normal, Histone antibody positive; Hypocomplementaemia, Joint swelling, Metabolic function test normal, Photosensitivity reaction, Protein urine present; Serology abnormal, Stomatitis, Systemic lupus erythematosus, Tenderness, Tunnel vision; Antinuclear antibody positive, Arthralgia, Double stranded DNA antibody positive, Full blood count normal, Histone antibody positive; Hypocomplementaemia, Joint swelling, Metabolic function test normal, Photosensitivity reaction, Protein urine present; Serology abnormal, Stomatitis, Systemic lupus erythematosus, Tenderness, Tunnel vision More
Systemic lupus erythematosus; This serious case was reported in a literature article and described t... Systemic lupus erythematosus; This serious case was reported in a literature article and described the occurrence of systemic lupus erythematosus in a 24-year-old female patient who received DTPa (DTaP vaccine) for prophylaxis. Literature Reference. Co-suspect products included Flu unspecified (Influenza vaccine) for prophylaxis. Additional patient notes included Patient with no past medical history. On an unknown date, the patient received DTaP vaccine and Influenza vaccine. On an unknown date, 2 days after receiving DTaP vaccine and Influenza vaccine, the patient experienced systemic lupus erythematosus (Verbatim: Systemic lupus erythematosus) (serious criteria GSK medically significant). The patient was treated with hydroxychloroquine and Steroids. The outcome of the systemic lupus erythematosus was resolving. The reporter considered the systemic lupus erythematosus to be possibly related to DTaP vaccine and Influenza vaccine. The company considered the systemic lupus erythematosus to be unrelated to DTaP vaccine and Influenza vaccine. Additional Information: GSK receipt date: 07-NOV-2025 Patient was a healthy 24-year-old female with no past medical history presenting to rheumatology clinic after two months of small joint pain, intermittent tunnel vision, photosensitivity, and mouth sores that started two days after receiving routine Tdap and Influenza vaccines for employment. Physical exam revealed swelling and tenderness of the left 2nd PIP and 5th right PIP. Her CBC and CMP were within normal limits, and her UA revealed 1+ protein. Serology showed hypocomplementemia, Anti SSA of 134, positive ANA 1:2560, dsDNA more than 365, RNP 6.8, and + anti-histone. Patient was diagnosed with systemic lupus erythematosus (SLE) was prescribed hydroxychloroquine and steroids for treatment. Patient was now doing well 3 months after starting treatment and was avoiding both the Tdap and flu vaccines. Patient's lack of past medical history and her timing of symptoms suggest that immune hyperactivation status post vaccine likely led to the development of SLE. Author could not know for sure which exact vaccine was the cause of the development of SLE in patient, this case highlights a rare adverse effect and the possibility of SLE after common vaccines.; Sender's Comments: A case of Systemic lupus erythematosus, 2 days after receiving DTaP vaccine and Influenza vaccine, in a 24-year-old female patient. Causal relation is indeterminate considering two vaccines given concomitantly. More
2873207 68 M 11/17/2025 COVID19
 MODERNA
 3052735
Flushing Flushing
continue to flush me out; This spontaneous case was reported by a consumer and describes the occurre... continue to flush me out; This spontaneous case was reported by a consumer and describes the occurrence of FLUSHING (continue to flush me out) in an elderly male patient who received mRNA-1283 (MNEXSPIKE PFS) (batch no. 3052735) for COVID-19 prophylaxis. The suspect product included Pre-filled Syringe injection (batch no. 3052735) for COVID-19 prophylaxis. No Medical History information was reported. On 16-Oct-2025, the patient received dose of mRNA-1283 (MNEXSPIKE PFS) (Intramuscular use) .2 milliliter. On an unknown date, the patient started Pre-filled Syringe (unknown route) at an unspecified dose. In 2025, the patient experienced FLUSHING (continue to flush me out). At the time of the report, FLUSHING (continue to flush me out) had not resolved. No concomitant medications were reported. No treatment information was provided. More
2873208 69 M 11/17/2025 COVID19
FLUX
 MODERNA
UNKNOWN MANUFACTURER

Follicular lymphoma recurrent, Underdose; Follicular lymphoma recurrent, Underdo... Follicular lymphoma recurrent, Underdose; Follicular lymphoma recurrent, Underdose More
lymph node that was about ready to cut off the blood supply to his right leg; Patient received lower... lymph node that was about ready to cut off the blood supply to his right leg; Patient received lower dose due to pharmacist who didn't even understand the difference (of the two vaccines); This spontaneous case was reported by a consumer and describes the occurrence of FOLLICULAR LYMPHOMA RECURRENT (lymph node that was about ready to cut off the blood supply to his right leg) in a 69-year-old male patient who received mRNA-1273.712 (SPIKEVAX 2024-2025 PFS) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. The suspect product included Pre-filled Syringe injection for COVID-19 prophylaxis. The non-company product included Influenza vaccine for an unknown indication. The patient's past medical history included Follicular lymphoma from 2019 to 2022 and CAR T-cell therapy (diagnosed 6 years ago). Previously administered products included for COVID-19 prophylaxis: moderna covid-19 vaccine (dose 1) in March 2021 and moderna covid-19 vaccine (dose 2) in March 2021; for Product used for unknown indication: Pneumonia (Pneumonia vaccine). Past adverse reactions to the above products included No adverse effect with Pneumonia, moderna covid-19 vaccine and moderna covid-19 vaccine. Concurrent medical conditions included Immunodeficiency (did not have any immune system). In November 2024, the patient received dose of mRNA-1273.712 (SPIKEVAX 2024-2025 PFS) (unknown route) 1 dosage form. On an unknown date, the patient started Pre-filled Syringe (unknown route) at an unspecified dose and dose of Influenza vaccine (unknown route) 1 dosage form. In November 2024, the patient experienced UNDERDOSE (Patient received lower dose due to pharmacist who didn't even understand the difference (of the two vaccines)). In December 2024, the patient experienced FOLLICULAR LYMPHOMA RECURRENT (lymph node that was about ready to cut off the blood supply to his right leg) (seriousness criterion medically significant). At the time of the report, FOLLICULAR LYMPHOMA RECURRENT (lymph node that was about ready to cut off the blood supply to his right leg) had resolved and UNDERDOSE (Patient received lower dose due to pharmacist who didn't even understand the difference (of the two vaccines)) outcome was unknown. The patient got a few vaccines that older people get, like pneumonia and a couple of other ones, but within 4 weeks, no vaccines were received by the patient. The only vaccines he had been getting besides those were the flu vaccine and COVID vaccines. It would not have been 4 weeks before because he always gets the flu vaccine in October or November. No relevant medical conditions. Before all the cancer, cell therapy, he was fine. Patient got all the COVID-19 vaccines in the past. He was on CAR-T therapy. He needed a completely different vaccine than everybody else and that, because of it, it changed him completely relative to everybody else. No concomitant medication was reported. He did not know how many doses he got. He got the initial 2 doses; it would have been Mar-2021; first of March and the last of March. It was reported that the patient might receive the first vaccination on 1-Mar-2021 and 2nd vaccination on 28-Mar-2021. According to his doctor, he needed 4 vaccines this season because he had CAR-T therapy. Because of this therapy, he was much more susceptible to COVID than most people because he did not have an immune system, and he was old. He got the lower dose last time because the pharmacist did not even understand the difference between the two vaccines. The patient did not have any immune system. Patient had been diagnosed with cancer many times, but his original diagnosis was 6 years ago. He started getting COVID vaccines as soon as they became available. Then in 2022, he got treatment and that got rid of it for 18 months. After that, it came back, got really bad, and then they got rid of it again; that was the main diagnosis in the meantime. Last December, he had a lymph node that was about ready to cut off the blood supply to his right leg. He got it taken care of quickly and, in the meantime, he got rid of all the cancer. He started CAR-T therapy in Apr-2025. He got 4 doses before that and since then he had 2 doses and had been due for another one. It was unknown if the patient experienced any additional symptoms/events. This case was linked to MOD-2025-789227 (Patient Link).; Reporter's Comments: Company comment: Causality for follicular lymphoma recurrent is assessed as not related considering underlying history of follicular lymphoma also with prior recurrences. The benefit-risk relationship of product is not affected by this report. More
2873209 F 11/17/2025 COVID19
 MODERNA
Illness Illness
has experienced sickness; This spontaneous case was reported by a consumer and describes the occurre... has experienced sickness; This spontaneous case was reported by a consumer and describes the occurrence of ILLNESS (has experienced sickness) in a female patient of an unknown age who received SPIKEVAX NOS (SPIKEVAX NOS) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of SPIKEVAX NOS (SPIKEVAX NOS) (Intramuscular use) 1 dosage form. On an unknown date, the patient experienced ILLNESS (has experienced sickness). At the time of the report, ILLNESS (has experienced sickness) outcome was unknown. The action taken with SPIKEVAX NOS (SPIKEVAX NOS) (Intramuscular use) was unknown. No concomitant medications provided by the reporter. The patient experienced sickness from previous Moderna vaccines. It was unknown if the patient experienced any additional symptoms/events. No treatment medications provided by the reporter. More
2873210 70 M CT 11/17/2025 COVID19
 PFIZER\BIONTECH
 NA4459
Body height, Disease recurrence, Generalised tonic-clonic seizure, Weight Body height, Disease recurrence, Generalised tonic-clonic seizure, Weight
Grand mal seizure; Grand mal seizure; This is a spontaneous report received from a Consumer or other... Grand mal seizure; Grand mal seizure; This is a spontaneous report received from a Consumer or other non HCP. A 70-year-old male patient received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), on 03Nov2025 as dose 1, 0.3 ml single (Lot number: NA4459) at the age of 70 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Epileptic" (ongoing), notes: He is epileptic and has been for 45 years or a long time/very controlled epileptic; "heart stent", start date: 2021 (unspecified if ongoing), notes: heart stent put in 3 or 4 years ago, thinks it was 4 years ago; "stage 4 lymphoma" (unspecified if ongoing), notes: roughly 7 or 8 years ago; "kidney transplant" (unspecified if ongoing), notes: received a kidney about 15 or 16 years ago. The patient took concomitant medications including anti rejection drugs for his kidney transplant, blood thinners. Vaccination history included: comirnaty (2024-2025 formula) (DOSE 1, 0.3 ML SINGLE; Lot: LM2215; left arm; grand mal seizure the next morning of vaccine), administration date: 06Sep2024, when the patient was 68-year-old, for COVID-19 immunization, reaction(s): "Grand mal seizure"; Flu shot (unknown manufacturer), for Immunization; Rsv shot (unknown manufacturer), for Immunization; Covid-19 vaccine (received since it came out for the last roughly 5 or 6 years; unknown manufacturer), for COVID-19 immunization, reaction(s): "fever that historically always get with the covid vaccine". The following information was reported: GENERALISED TONIC-CLONIC SEIZURE (hospitalization), DISEASE RECURRENCE (hospitalization) all with onset 05Nov2025, outcome "unknown" and all described as "Grand mal seizure". The patient was hospitalized for generalised tonic-clonic seizure, disease recurrence (start date: 05Nov2025, discharge date: 07Nov2025, hospitalization duration: 3 day(s)). The patient underwent the following laboratory tests and procedures: Body height: little over 5'11'', notes: close to 6 feet; Weight: 200 to 202. Therapeutic measures were taken as a result of generalised tonic-clonic seizure included extra doses of Dilantin. Clinical course: The patient had another grand mal seizure that occurred Wednesday first thing in the morning on 05Nov2025. He received the Pfizer covid 19 vaccine last Monday 03Nov2025. He went to the hospital and same thing happened where he had a grand mal seizure at home and then a very bad grand mal seizure while he was admitted to the hospital. He was discharged from the hospital Friday afternoon, so states he was admitted for about 3 days. No investigations. More
✓
2873211 F 11/17/2025 COVID19
 PFIZER\BIONTECH
Conjunctival haemorrhage, Toothache Conjunctival haemorrhage, Toothache
optical reactions to the shot, had symptoms in the white part of her eye like blood vessels were bro... optical reactions to the shot, had symptoms in the white part of her eye like blood vessels were broken; oral reaction where her teeth were hurting; This is a spontaneous report received from a Consumer or other non HCP. A female patient received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: CONJUNCTIVAL HAEMORRHAGE (non-serious), outcome "unknown", described as "optical reactions to the shot, had symptoms in the white part of her eye like blood vessels were broken"; TOOTHACHE (non-serious), outcome "unknown", described as "oral reaction where her teeth were hurting". Additional information: optical reactions to the shot, had symptoms in the white part of her eye like blood vessels were broken. Had oral reaction where her teeth were hurting. Had reaction about 24 hours after where she got real sick. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained. More
2873212 F SC 11/17/2025 COVID19
 PFIZER\BIONTECH
COVID-19, SARS-CoV-2 test COVID-19, SARS-CoV-2 test
that's probably when we had COVID before. This is our second COVID, and we had all the vaccines... that's probably when we had COVID before. This is our second COVID, and we had all the vaccines except for the very last one... And it was Pfizer.; This is a spontaneous report received from a Consumer or other non HCP, Program ID. An 81-year-old female patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 nos (DOSE NUMBER UNKNOWN, SINGLE), for Covid-19 immunization. The following information was reported: COVID-19 (non-serious), outcome "unknown", described as "that's probably when we had COVID before. This is our second COVID, and we had all the vaccines except for the very last one... And it was Pfizer.". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of covid-19. Additional information: The patient had then been transferred to [withheld] for reimbursement assistance. Once the call was transferred, the patient, stated, she was on Paxlovid her husband and she both have COVID, and he probably got it a couple of days before she did. So, she assuming she caught it from him. Then she didn't test, until it was Thursday of last week, she believes, and when she tested both positive. So, then both called our doctor and told them, you know, that both had COVID, and they called in a prescription. We go to different doctors. So, his doctor called his in and her doctor called mine in. Well, he went to the pharmacy and got his. Then it was several hours later, and the pharmacy called her, and they said that they were out of it when her doctor sent her prescription in so finally, they got it filled, and she went to pick it up and when she picked it up, they charged me 47 dollars. When asked for the date her medication was purchased, patient stated yes, it was on 06November. After advising that an enrollment would need to be completed, patient would have to take more Paxlovid if she get sicker or don't get well? After advising of the options for enrollment, after advising patient that an account created in January 2024 was located for her, patient stated, okay, that's probably when we had COVID before. This is our second COVID, and we had all the vaccines except for the very last one. And it was Pfizer. You probably have information on me because we've we had the Pfizer vaccine, her husband and she when offered to be transferred to the Drug Safety Unit, patient stated, well, she thinks it's working, we're better. Okay, she will. She was about worn out now, though, but it won't be much longer. Patient continued to state patient started out with a sore throat, but my husband, he didn't have a sore throat, and he doesn't have one now. But she has still got a terrible sore throat. Her throat was very red. After transferring to the Drug safety Unit patient stated, just pray for us to get well and this Paxlovid to work. More
2873213 M NC 11/17/2025 FLUX
 UNKNOWN MANUFACTURER
Malaise, Nausea, Pain, Pyrexia Malaise, Nausea, Pain, Pyrexia
significant body pain; fever; Nausea; general malaise; Initial information received on 07-Nov-2025 r... significant body pain; fever; Nausea; general malaise; Initial information received on 07-Nov-2025 regarding an unsolicited valid non-serious case received from a consumer/non-healthcare professional. This case involves Adult male patient (185.42 cm and 79.55 kg) who had significant body pain, fever, nausea and general malaise after receiving influenza vaccine. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. At the time of the event, the patient had ongoing Drug hypersensitivity with Carbamazepine 100 Mg Tab Chew, Tegretol 200 Mg Tablet, Sucralfate 1 Gm Tablet, Captopril 25 Mg Tablet, Honey Bee Venom Protein Vl, Sulfamethoxazole-Tmp Ss Tablet, Sulfacetamide 10% Eye Drops, Lisinopril 10 Mg Tablet, Lisinopril 10 Mg Tablet, Levofloxacin 250 Mg Tablet. Concomitant medications included epinephrine; normal saline; fluticasone propionate; methocarbamol; zyrtec [cetirizine hydrochloride]; percocet [oxycodone hydrochloride;paracetamol]; sodium chloride; hydrocodone bitartrate, paracetamol (hydrocodone/acetaminophen); losartan potassium; omeprazole (protonix); agalsidase beta (fabrazyme); diphenhydramine hydrochloride (diphenhydramine); gabapentin; aspirin [acetylsalicylic acid]; ibuprofen; paracetamol (tylenol extra-strength); and finasteride. On an unknown date, the patient received unknown dose of suspect influenza vaccine (Unknown strength, formulation, lot and expiry date) produced by unknown manufacturer via unknown route in unknown administration site for Prophylactic vaccination (Immunisation) On an unknown date the patient developed significant body pain (pain), fever (pyrexia), nausea and general malaise (malaise) (unknown latency) following the administration of influenza vaccine. Action taken was not applicable. It was not reported if the patient received corrective treatment for all the events. At time of reporting, the outcome was Unknown for all the events.; Sender's Comments: US-SA-2025SA305737: More
2873214 79 F NY 11/17/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR

Discomfort, Injection site swelling, Myalgia, Pain in extremity, Rhinorrhoea; Sl... Discomfort, Injection site swelling, Myalgia, Pain in extremity, Rhinorrhoea; Sleep disorder More
discomfort; muscle pain from her waist down the left side of her body; swelling at the injection sit... discomfort; muscle pain from her waist down the left side of her body; swelling at the injection site; sore arm; runny nose; difficulty sleeping due to the muscle pain and noted that she must sleep in a certain position due to the pain; Initial information received on 10-Nov-2025 regarding an unsolicited valid non-serious case (along with live follow-up processed together with csd dated: 10-Nov-2025) received from a patient. This case involves a 79 years old female patient who had difficulty sleeping due to the muscle pain and noted that she must sleep in a certain position due to the pain, discomfort, runny nose, muscle pain from her waist down the left side of her body, sore arm and swelling at the injection site after receiving Influenza Usp Trival A-B High Dose Subvirion Vaccine [Fluzone Hd]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 21-Oct-2025, the patient received 0.5 ml dose of suspect Influenza Usp Trival A-B High Dose Subvirion Vaccine, Suspension for injection in pre-filled syringe (lot number and expiry date not reported) strength: high dose, via unknown route in the left arm for Influenza [Immunisation]. Information on the batch number was requested corresponding to the one at time of event occurrence. On an unknow date In Oct-2025 the patient muscle pain from her waist down the left side of her body (myalgia) and discomfort (latency: few days approximately). On an unknown date In 2025 the patient had runny nose (rhinorrhoea), difficulty sleeping due to the muscle pain and noted that she must sleep in a certain position due to the pain (sleep disorder due to a general medical condition), sore arm (pain in extremity) and swelling at the injection site (vaccination site swelling) (latency: few days approximately). It is reported" Neither caller nor spouse have contacted their healthcare provider. However, they both have an appointment scheduled next week for their routine 6 month appointments". Action taken was not applicable. The patient was treated with Acetylsalicylic acid (Baby aspirin) for all the events. At time of reporting, the outcome was Unknown for all the events.; Sender's Comments: US-SA-2025SA337793:02718195, for patient (wife) More
2873219 1.92 F OK 11/17/2025 UNK
 UNKNOWN MANUFACTURER
 No batch number
Hypersensitivity, Ludwig angina, Urticaria Hypersensitivity, Ludwig angina, Urticaria
Anginas on her face; Minor allergy after the administration of Flucelvax; Hives on her face; This sp... Anginas on her face; Minor allergy after the administration of Flucelvax; Hives on her face; This spontaneous case, initially received on 03-Nov-2025, was reported by a health professional and concerns an child female patient. Medical history and concomitant medications was reported as unknown. Administration of company suspect drug: On an unknown date in Oct-2023, the patient received Flucelvax (TIV) for unknown indication, Dose regimen: not reported, route of administration: not reported, Lot number: No batch number available and would be requested upon follow up. No additional suspect drugs. Adverse reactions/events and outcomes: On an unknown date, the patient experienced Anginas on her face (Medically Significant, outcome: Unknown), Hives on her face (outcome: Unknown), Minor allergy after the administration of Flucelvax (outcome: Unknown). Case was upgraded to serious upon company assessment of the reported event (Anginas on her face) clinical significance. The physician called and asked about a list of ingredients for the Flucelvax vaccine. The physician stated that a child had experienced a minor allergy after the administration of Flucelvax. The physician specified that the child had developed hives and anginas on her face within 5 to 10 minutes after the administration. The physician referred that Flucelvax was the only vaccine the child had received that day. The physician provided the NDC (sic!) Number and asked about the Gelatin constituent and requested a list of vaccine constituents. The physician informed that she was the mother of the child, and the HCP who administered the vaccine was another physician who was no longer following the case. Flucelvax (TIV) action taken: Not Applicable Treatment measures associated with event: Unknown Reporter's assessment: The reporter did not provide the seriousness and causality of assessment for the events.; Reporter's Comments: Due to the spontaneous nature of the case, all events are considered related for the reporting purposes. Related for all events considering close temporal relationship ( 5 to 10 minutes after the vaccine administration) and biological plausibility. More
2873220 0.33 M CA 11/17/2025 DTAPIPVHIB
DTAPIPVHIB
PNC13
PNC13
RV1
RV1
PNC20
PNC20
RV1
RV1
SMALL
SMALL
 SANOFI PASTEUR
SANOFI PASTEUR
PFIZER\WYETH
PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
PFIZER\WYETH
PFIZER\WYETH
GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
EMERGENT BIOSOLUTIONS
EMERGENT BIOSOLUTIONS
 UK345AB
UK345AB
MA24A3
MA24A3
J757K
J757K
MA2483
MA2483
J757K
J757K
UK345AB
UK345AB
Irritability, Seizure, Somnolence, Tremor; Fatigue, Pallor, Seizure, Somnolence,... Irritability, Seizure, Somnolence, Tremor; Fatigue, Pallor, Seizure, Somnolence, Tremor; Irritability, Seizure, Somnolence, Tremor; Fatigue, Pallor, Seizure, Somnolence, Tremor; Irritability, Seizure, Somnolence, Tremor; Fatigue, Pallor, Seizure, Somnolence, Tremor; Irritability, Seizure, Somnolence, Tremor; Fatigue, Pallor, Seizure, Somnolence, Tremor; Irritability, Seizure, Somnolence, Tremor; Fatigue, Pallor, Seizure, Somnolence, Tremor; Irritability, Seizure, Somnolence, Tremor; Fatigue, Pallor, Seizure, Somnolence, Tremor More
My son had his 4month vaccines on 11/17/2025. A that same day my son got a reactions about 10mins af... My son had his 4month vaccines on 11/17/2025. A that same day my son got a reactions about 10mins after his shots. The nurse and my sons Doctor gave us the final paperwork, that we were ready to go. So right after his shots I put my sons cloths back on everything was normal he was fine etc. I did notice he was a little sleepy so I thought nothing much about it. I gave him his milk mean while my husband was putting his pants on. Once my husband was done he was putting him in his carseat but he did have his eyes clothes but woke up once we put him in his carseat he got a little fussy. I went over to give him his milk, that's when I notice my son's left arm was shaking that's when I got worried because that is nothing he does. that's when I picked him up from his carseat in the meanwhile I told my husband to call the doctor back into the room we were in and once I picked him up he could of burly open his eyes. My son was super drowsy that's when Doctor came in and told me to take off his clothes he woke up once I laid him down on the bed. Doctor checked his heart rate. It was a little hard to read it. During when doctor was checking him she told one of the nurses to give him Tylenol 2.7ml was what she gave him so he would not get any fever. But what Doctor mentioned to me was he was most likely a slight seizer. That's what I don't want to believe but the way he reacted was very scary and horrible moment. Doctor told me to wait 20 more mins before we should leave so she can monitor him. The 20mins have passed he did get better but we just don't know for his 6month this vaccine should be given to him. More
2873221 30 M HI 11/17/2025 FLU3
FLU3
 SANOFI PASTEUR
SANOFI PASTEUR
 U8848AA
U8848AA
Brain fog, Condition aggravated, Fatigue, Insomnia, Poor quality sleep; Post-acu... Brain fog, Condition aggravated, Fatigue, Insomnia, Poor quality sleep; Post-acute COVID-19 syndrome More
Aggravated post covid 19 vaccine syndrome symptoms: increased chronic fatigue, recurrence of brain f... Aggravated post covid 19 vaccine syndrome symptoms: increased chronic fatigue, recurrence of brain fog, poor sleep / temporary insomnia for several weeks (up till 3 am or later several nights laying in bed). More
2873222 58 M VA 11/17/2025 FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.
 948419
948419
Blindness, Computerised tomogram head, Glycosylated haemoglobin, Ischaemic strok... Blindness, Computerised tomogram head, Glycosylated haemoglobin, Ischaemic stroke, Lipids; Magnetic resonance imaging head, Occipital lobe stroke More
vision loss/ ischemic stroke/acute occipital CVS vision loss/ ischemic stroke/acute occipital CVS
✓ ✓
2873223 77 F SC 11/17/2025 FLU3
 SANOFI PASTEUR
 u8859ba
Blister Blister
Patient described blisters on her head and 2 in her mouth that started 2 days after vaccine was admi... Patient described blisters on her head and 2 in her mouth that started 2 days after vaccine was administered. She states she did not change detergents, washes, etc and can only attribute the reaction to possibly being caused by the vaccine. She did not reach out to her doctor or seek medical attention. She states that she did not treat with any medication. She states that they have just now resolved on their own. More
2873234 68 F AZ 11/17/2025 FLU3
FLU3
FLU3
 SEQIRUS, INC.
SEQIRUS, INC.
SEQIRUS, INC.


Blood test abnormal, Burning sensation, Chest discomfort, Dyspnoea, Electrocardi... Blood test abnormal, Burning sensation, Chest discomfort, Dyspnoea, Electrocardiogram normal; Feeling jittery, Feeling of body temperature change, Muscle tightness, Neuralgia, Sleep disorder; Tinnitus, X-ray normal More
Nerve pain and burning from head to toe. Increased ear ringing. The nerve burning worsened at nigh... Nerve pain and burning from head to toe. Increased ear ringing. The nerve burning worsened at night, with muscle tightness, jittery feeling and chest pressure. Some shortness of breath. Fluctuating feeling hot and cold. I woke up at night with the nerves in my back burning even worse. I had problems sleeping. I went to the ER on Nov. 9th. They ran blood work, did an EKG, Chest X-ray and gave me fluids, a muscle relaxer and Tylenol. All my tests were normal, except one blood level for muscles was off by a point. More
2873236 23 F FL 11/17/2025 FLU3
 SANOFI PASTEUR
 U8823BA
Injection site discolouration, Pain in extremity Injection site discolouration, Pain in extremity
Patient still has a very sore arm, 3 and a half weeks after receiving her injection. It is very pain... Patient still has a very sore arm, 3 and a half weeks after receiving her injection. It is very painful despite icing and using pain relievers. She does not have restrictions in range of motion, nor does she have any numbness/tingling. Patient says the injection site is still a little black/blue, but the injection site never appeared abnormal (no bubbling/pooling of blood directly under the skin). Unfortunately, the patient's insurance has recently changed and she no longer has a primary care provider. She is going to consider going to an urgent care to be evaluated. More
2873237 79 M PR 11/17/2025 FLU3
PNC20
 SANOFI PASTEUR
PFIZER\WYETH
 U8855CA
MA2488
Pain in extremity, Peripheral swelling; Pain in extremity, Peripheral swelling Pain in extremity, Peripheral swelling; Pain in extremity, Peripheral swelling
Swelling an pain on right arm during the night. Treatment: Tylenol or Panadol, Advil Dual Action, Al... Swelling an pain on right arm during the night. Treatment: Tylenol or Panadol, Advil Dual Action, Alcoholado, Lidocaine Patches. tonight he is going to start using Arnica gel. More
2873238 M CO 11/17/2025 COVID19
 MODERNA
 8146751
Flushing, Pruritus Flushing, Pruritus
Approximately 5 min after inj, patient became flushed and verbally reported an itching sensation. rp... Approximately 5 min after inj, patient became flushed and verbally reported an itching sensation. rph administered 10 mL (25 mg) of benadryl to patient orally via liquid syringe. patient was monitored for 30 minutes and reported symptoms had subsided and he no longer appeared flushed or felt itchy More
2873239 55 F CO 11/17/2025 FLU3
PNC20
 SANOFI PASTEUR
PFIZER\WYETH
 U8864AA
MA2506
Erythema, Pain in extremity, Peripheral swelling; Erythema, Pain in extremity, P... Erythema, Pain in extremity, Peripheral swelling; Erythema, Pain in extremity, Peripheral swelling More
Red arm, swollen, pain, middle of the left arm Red arm, swollen, pain, middle of the left arm
2873242 38 F WA 11/17/2025 COVID19
COVID19
 MODERNA
MODERNA

Disorientation, Dizziness, Nausea, Pain, Pain in extremity; Paraesthesia, Vomiti... Disorientation, Dizziness, Nausea, Pain, Pain in extremity; Paraesthesia, Vomiting More
Pain and tingling spreading through injection arm, across torso at first 10-15 minutes. Disorientati... Pain and tingling spreading through injection arm, across torso at first 10-15 minutes. Disorientation, dizziness 15-25. nausea, vomiting 25-40. Two Benadryl taken at 20minutes, effects lessened at 55minutes. More
2873243 39 F IL 11/17/2025 FLU3
FLU3
 GLAXOSMITHKLINE BIOLOGICALS
GLAXOSMITHKLINE BIOLOGICALS
 34N52
34N52
Chest X-ray, Chest discomfort, Dyspnoea, Electrocardiogram normal, Haematemesis;... Chest X-ray, Chest discomfort, Dyspnoea, Electrocardiogram normal, Haematemesis; Nausea More
On Sunday after her flu vaccine, patient reports nausea, vomiting and chest pressure. All subsided b... On Sunday after her flu vaccine, patient reports nausea, vomiting and chest pressure. All subsided by Monday except the chest pressure/tightness. On Tuesday went to an urgent care and had a CXR and EKG which are reported as normal. On Wed reports she had some SOB and by Thursday symptoms had resolved. No other symptoms were reported. Patient reports never having an event like this post flu vaccine before. More
2873259 76 F WA 11/17/2025 COVID19
COVID19
 PFIZER\BIONTECH
PFIZER\BIONTECH
 NA0738
NA0738
Atrial fibrillation, Back pain, Blood pressure increased, Blood test, Electrocar... Atrial fibrillation, Back pain, Blood pressure increased, Blood test, Electrocardiogram; Heart rate increased, Immediate post-injection reaction, Left ventricular enlargement, Myalgia More
Extreme debillitating muscular pain in back, hips and arms and legs Increased Heart rate and blood p... Extreme debillitating muscular pain in back, hips and arms and legs Increased Heart rate and blood pressure. Immediate onset AFIB lasting Sept 25 through current date 11'/11/2025introduced Metroprolol and Pradaxa blood thinner, enlarged left ventrical. More
2872967 3 M HI 11/16/2025 UNK
 UNKNOWN MANUFACTURER
Injection site erythema, Injection site oedema, Injection site pain Injection site erythema, Injection site oedema, Injection site pain
moderate amount of local edema and erythema to injection site, about 6inch diameter encompassing sho... moderate amount of local edema and erythema to injection site, about 6inch diameter encompassing shoulder. started several hours after injection. reported pain to the site. in ED provided with ibuprofen and tylenol More
2872970 65 F MI 11/16/2025 COVID19
 NOVAVAX
 6024MF0 14A
Hypotonia, Injection site pain, Mobility decreased, Muscular weakness Hypotonia, Injection site pain, Mobility decreased, Muscular weakness
When I awoke on the third day after the shot, I could not use my left arm. It was limp. I could not ... When I awoke on the third day after the shot, I could not use my left arm. It was limp. I could not lift it. I forced myself to try to use it in the following days and it got slightly better, however, it was very painful in the area above my elbow. To this day, over a year later, my upper left arm is not as strong and has been so painful I received two steroid shots to ease the pain. More
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